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Article
April 1977

Lattice Corneal DystrophyReport of an Unusual Case

Author Affiliations

From the Departments of Ophthalmology and Pathology, University of Pennsylvania, the Laboratory of Ophthalmic Pathology, Scheie Eye Institute and Hospital, Philadelphia, and the Ophthalmic Pathology Division, Armed Forces Institute of Pathology, Washington, DC.

Arch Ophthalmol. 1977;95(4):651-655. doi:10.1001/archopht.1977.04450040117018
Abstract

• The clinical, histochemical, light and electron microscopic evaluation of a case of lattice corneal dystrophy, appears clinically as an atypical granular dystrophy. There is structural and histochemical differentiation of the two dystrophies. Electron microscopy is often an invaluable aid in establishing a definitive diagnosis. The possible sources of the filamentous material found in lattice corneal dystrophy are discussed. It seems that not only keratocytes, but also corneal epithelial cells, occasionally may have the ability to elaborate the abnormal material that is considered to be amyloid in nature.

(Arch Ophthalmol 95:651-655, 1977)

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